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Antidecubito gomito naturale

EUDAMED

Class I (EU MDR)

Ref 702/G

by G.l.o. Srl

Identity

Device Name
Antidecubito gomito naturale EUDAMED
Model / Reference
702/G EUDAMED

Identifiers

Primary DI / UDI-DI
08051070434037 EUDAMED
Basic UDI-DI
805107043702GUW EUDAMED
EMDN Code
V0811 HEEL, ELBOW AND KNEE ANTI-DECUBITUS PROTECTION AIDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Antidecubito gomito naturale by G.l.o. Srl — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
G.l.o. Srl
EUDAMED SRN
IT-MF-000018554

Sources (1)

  • EUDAMED 9617c9e6-95d0-415b-be4c-0696fdaeba61 61 fields · synced Jun 18, 2026